Package 0641-6178-01

Brand: octreotide acetate

Generic: octreotide acetate
NDC Package

Package Facts

Identity

Package NDC 0641-6178-01
Digits Only 0641617801
Product NDC 0641-6178
Description

1 VIAL, MULTI-DOSE in 1 CARTON (0641-6178-01) / 5 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2005-04-08
Brand octreotide acetate
Generic octreotide acetate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "efa5d8e8-57ab-4b56-b8d7-f856ea97404c", "openfda": {"unii": ["75R0U2568I"], "rxcui": ["312068", "312069", "312070", "312071", "314152"], "spl_set_id": ["9502860d-0261-4d69-a4be-827a5376d356"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (0641-6178-01)  / 5 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "0641-6178-01", "marketing_start_date": "20050408"}], "brand_name": "Octreotide Acetate", "product_id": "0641-6178_efa5d8e8-57ab-4b56-b8d7-f856ea97404c", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Somatostatin Analog [EPC]", "Somatostatin Receptor Agonists [MoA]"], "product_ndc": "0641-6178", "generic_name": "Octreotide Acetate", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Octreotide Acetate", "active_ingredients": [{"name": "OCTREOTIDE ACETATE", "strength": "1000 ug/mL"}], "application_number": "ANDA076330", "marketing_category": "ANDA", "marketing_start_date": "20050408", "listing_expiration_date": "20271231"}